NOP56 NOP56 ribonucleoprotein

Information
Symbol
NOP56
Type
protein-coding
Description
NOP56 ribonucleoprotein
Entrez Gene ID
10528
Genome
hg19
Position
chr20:2,633,278-2,639,039
Genome
hg38
Position
chr20:2,652,632-2,658,393
MIM
614154 OMIM
HGNC
HGNC:15911 HGNC
Ensembl
ENSG00000101361 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 12
Likely benign 0 26
Uncertain significance 0 58
Ranking
ClinVar
0
0
4
80
14
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM NOL5A
SYNONYM SCA36
MIM 614154 OMIM
HGNC HGNC:15911 HGNC
Ensembl ENSG00000101361 Ensembl
AllianceGenome HGNC:15911
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000329276.10 hg38 chr20 2,652,632 2,658,393 5,762
ENST00000329276.10 hg19 chr20 2,633,278 2,639,039 5,762
Genome browser